CO6541606A2 - ESPIROINDOLINONA- PIRROLIDINAS - Google Patents

ESPIROINDOLINONA- PIRROLIDINAS

Info

Publication number
CO6541606A2
CO6541606A2 CO12086101A CO12086101A CO6541606A2 CO 6541606 A2 CO6541606 A2 CO 6541606A2 CO 12086101 A CO12086101 A CO 12086101A CO 12086101 A CO12086101 A CO 12086101A CO 6541606 A2 CO6541606 A2 CO 6541606A2
Authority
CO
Colombia
Prior art keywords
pirrolidinas
espiroindolinona
compounds
nicancerous
esters
Prior art date
Application number
CO12086101A
Other languages
Spanish (es)
Inventor
David Joseph Bartkovitz
Xin-Jie Chu
Zhuming Zhang
Jing Zhang
Nan Jiang
Bradford James Graves
Qingjie Ding
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of CO6541606A2 publication Critical patent/CO6541606A2/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10Spiro-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Indole Compounds (AREA)

Abstract

Se proporcionan compuestos de la fórmula (I)en la que X, Y y de R1 a R8 tienen los significados aquí definidos, junto con, los enantiómeros, las sales y los esteres farmacéuticamente aceptables de los mismos. Estos compuestos son útiles como agentes nticancerosos.Compounds of the formula (I) are provided in which X, Y and R1 to R8 have the meanings defined herein, together with, the pharmaceutically acceptable enantiomers, salts and esters thereof. These compounds are useful as nicancerous agents.

CO12086101A 2009-12-02 2012-05-24 ESPIROINDOLINONA- PIRROLIDINAS CO6541606A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US26579209P 2009-12-02 2009-12-02
US38805410P 2010-09-30 2010-09-30

Publications (1)

Publication Number Publication Date
CO6541606A2 true CO6541606A2 (en) 2012-10-16

Family

ID=43608656

Family Applications (1)

Application Number Title Priority Date Filing Date
CO12086101A CO6541606A2 (en) 2009-12-02 2012-05-24 ESPIROINDOLINONA- PIRROLIDINAS

Country Status (26)

Country Link
US (1) US8088815B2 (en)
EP (1) EP2507243B1 (en)
JP (1) JP5647262B2 (en)
KR (1) KR101418191B1 (en)
CN (1) CN102741257B (en)
AR (1) AR079226A1 (en)
AU (1) AU2010326855B2 (en)
BR (1) BR112012012872A2 (en)
CA (1) CA2781823A1 (en)
CL (1) CL2012001405A1 (en)
CO (1) CO6541606A2 (en)
CR (1) CR20120259A (en)
EC (1) ECSP12011945A (en)
ES (1) ES2543468T3 (en)
HK (1) HK1173720A1 (en)
IL (1) IL220010A (en)
MA (1) MA33976B1 (en)
MX (1) MX2012006260A (en)
MY (1) MY160596A (en)
NZ (1) NZ600024A (en)
PE (1) PE20121334A1 (en)
RU (1) RU2571100C2 (en)
SG (1) SG181465A1 (en)
TW (1) TW201129571A (en)
WO (1) WO2011067185A1 (en)
ZA (1) ZA201204036B (en)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5649825B2 (en) * 2007-01-31 2015-01-07 デイナ ファーバー キャンサー インスティチュート,インコーポレイテッド Stabilized p53 peptides and methods of use thereof
KR20160061439A (en) 2007-03-28 2016-05-31 프레지던트 앤드 펠로우즈 오브 하바드 칼리지 Stitched polypeptides
UA107814C2 (en) 2009-11-12 2015-02-25 Дзе Ріджентс Оф Дзе Юніверсіті Оф Мічіган Spiro-oxindoles antagonists mdm 2
US20110118283A1 (en) * 2009-11-17 2011-05-19 Qingjie Ding Substituted Pyrrolidine-2-Carboxamides
US8288431B2 (en) * 2010-02-17 2012-10-16 Hoffmann-La Roche Inc. Substituted spiroindolinones
JO2998B1 (en) 2010-06-04 2016-09-05 Amgen Inc Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer
KR102104762B1 (en) 2010-08-13 2020-04-24 에일러론 테라퓨틱스 인코포레이티드 Peptidomimetic macrocycles
US20120046306A1 (en) * 2010-08-18 2012-02-23 David Joseph Bartkovitz Substituted Heteroaryl Spiropyrrolidine MDM2 Antagonists
WO2012065022A2 (en) 2010-11-12 2012-05-18 The Regents Of The University Of Michigan Spiro-oxindole mdm2 antagonists
CA2829188C (en) 2011-03-10 2016-10-18 Daiichi Sankyo Company, Limited Dispiropyrrolidine derivatives
KR101688268B1 (en) 2011-05-11 2016-12-20 더 리젠츠 오브 더 유니버시티 오브 미시간 Spiro-oxindole mdm2 antagonists
MX352672B (en) 2011-09-27 2017-12-04 Amgen Inc Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer.
KR20140100937A (en) 2011-10-18 2014-08-18 에일러론 테라퓨틱스 인코포레이티드 Peptidomimetic macrocycles
CN104144695A (en) 2012-02-15 2014-11-12 爱勒让治疗公司 Triazole-crosslinked and thioether-crosslinked peptidomimetic macrocycles
CN107216380A (en) 2012-02-15 2017-09-29 爱勒让治疗公司 Peptidomimetic macrocyclic compound
TWI586668B (en) 2012-09-06 2017-06-11 第一三共股份有限公司 Crystals of dispiropyrrolidine derivative
KR20150082307A (en) 2012-11-01 2015-07-15 에일러론 테라퓨틱스 인코포레이티드 Disubstituted amino acids and methods of preparation and use thereof
AU2013361694B2 (en) 2012-12-20 2017-10-26 Merck Sharp & Dohme Corp. Substituted imidazopyridines as HDM2 inhibitors
US11407721B2 (en) 2013-02-19 2022-08-09 Amgen Inc. CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer
WO2014134201A1 (en) * 2013-02-28 2014-09-04 Amgen Inc. A benzoic acid derivative mdm2 inhibitor for the treatment of cancer
EP2970237B1 (en) 2013-03-14 2017-09-27 Amgen Inc. Heteroaryl acid morpholinone compounds as mdm2 inhibitors for the treatment of cancer
JOP20200296A1 (en) 2013-06-10 2017-06-16 Amgen Inc Processes of Making and Crystalline Forms of a MDM2 Inhibitor
CN103342672B (en) * 2013-07-02 2015-12-23 扬州大学 The novel synthesis of substituted pyrrolidin-2-ketone
SG10201913742TA (en) 2014-04-17 2020-03-30 Univ Michigan Regents Mdm2 inhibitors and therapeutic methods using the same
EP3164401B1 (en) 2014-07-03 2018-12-26 Boehringer Ingelheim International GmbH New spiro[3h-indole-3,2´-pyrrolidin]-2(1h)-one compounds and derivatives as mdm2-p53 inhibitors
US9701685B2 (en) 2014-08-18 2017-07-11 Hudson Biopharma Inc. Spiropyrrolidines as MDM2 inhibitors
BR112017005598A2 (en) 2014-09-24 2017-12-12 Aileron Therapeutics Inc peptidomimetic macrocycles and their uses
SG10201902598VA (en) 2014-09-24 2019-04-29 Aileron Therapeutics Inc Peptidomimetic macrocycles and formulations thereof
EP3294318A4 (en) 2015-03-20 2019-04-03 Aileron Therapeutics, Inc. Peptidomimetic macrocycles and uses thereof
RU2629750C2 (en) * 2015-04-09 2017-09-01 Ян Андреевич Иваненков NEW DISPIRO-INDOLINONES, MDM2/p53 INTERACTION INHIBITORS, METHOD FOR PRODUCTION AND APPLICATION
WO2017044633A1 (en) 2015-09-10 2017-03-16 Aileron Therapeutics, Inc. Peptidomimetic macrocycles as modulators of mcl-1
UA123905C2 (en) 2015-10-09 2021-06-23 Бьорінгер Інгельхайм Інтернаціональ Гмбх Spiro[3h-indole-3,2´-pyrrolidin]-2(1h)-one compounds and derivatives as mdm2-p53 inhibitors
GB201603779D0 (en) * 2016-03-04 2016-04-20 Mission Therapeutics Ltd Novel compounds
RU2021102253A (en) * 2016-04-06 2021-03-03 Дзе Риджентс Оф Дзе Юниверсити Оф Мичиган DESTRUCTORS OF MDM2 PROTEIN
CN105949221B (en) * 2016-05-11 2017-08-25 湖南科技大学 Ketone derivatives of a kind of indoles containing spiral shell 2 and preparation method thereof and it is used as the application of cancer therapy drug
WO2017201449A1 (en) 2016-05-20 2017-11-23 Genentech, Inc. Protac antibody conjugates and methods of use
JP6848047B2 (en) * 2016-08-08 2021-03-24 フェイ シアオ, Spiroindron polyethylene glycol carbonate-based compound and its composition, preparation method and its use
EP3511334A1 (en) * 2018-01-16 2019-07-17 Adamed sp. z o.o. 1,2,3',5'-tetrahydro-2'h-spiro[indole-3,1'-pyrrolo[3,4-c]pyrrole]-2,3'-dione compounds as therapeutic agents activating tp53
RU2730287C1 (en) * 2019-08-30 2020-08-21 Федеральное государственное бюджетное образовательное учреждение высшего образования "Московский государственный университет имени М.В. Ломоносова" (МГУ) Novel 2',5'-diarylspiro[indole-3,3'-pyrrolidine]-2(1h)-ones and a method for production thereof
GB201919219D0 (en) 2019-12-23 2020-02-05 Otsuka Pharma Co Ltd Cancer biomarkers
CA3181715A1 (en) 2020-08-27 2022-03-03 Otsuka Pharmaceutical Co., Ltd. Biomarkers for cancer therapy using mdm2 antagonists
WO2022159644A1 (en) * 2021-01-23 2022-07-28 Newave Pharmaceutical Inc. Spirocyclic mdm2 modulator and uses thereof
GB202103080D0 (en) 2021-03-04 2021-04-21 Otsuka Pharma Co Ltd Cancer biomarkers
CN115215872A (en) * 2021-04-15 2022-10-21 中国科学院上海药物研究所 Small molecule compound with substituted phenyl spiro [ indoline-3, 3' -pyrrolidine ] structure
CN113387957B (en) * 2021-06-09 2022-08-09 江苏亚尧生物科技有限公司 Spirocyclic indolone-pyrrolidine carbonate compound and composition, preparation method and application thereof
WO2023056069A1 (en) 2021-09-30 2023-04-06 Angiex, Inc. Degrader-antibody conjugates and methods of using same
WO2023086400A1 (en) * 2021-11-12 2023-05-19 Enanta Pharmaceuticals, Inc. Novel spiropyrrolidine derived antiviral agents
US11993600B2 (en) 2021-12-08 2024-05-28 Enanta Pharmaceuticals, Inc. Saturated spirocyclics as antiviral agents
CN114773327B (en) * 2022-04-18 2023-08-18 广东优康精细化工有限公司 Preparation method of penthiopyrad intermediate

Family Cites Families (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2759935A (en) * 1953-02-18 1956-08-21 Bristol Lab Inc Substituted 3-phenyloxindoles
US3441570A (en) * 1966-01-20 1969-04-29 Parke Davis & Co 3-tertiary aminoalkylamino-3-phenyl oxindole compounds
US3686210A (en) * 1970-01-13 1972-08-22 American Home Prod 2-acylamido-3-aryl-3h-indol-3-ol esters and related compounds
US4020179A (en) * 1975-05-15 1977-04-26 Richardson-Merrell Inc. 7-Substituted-2-indolinones
JPS55129284A (en) 1979-03-27 1980-10-06 Shionogi & Co Ltd 3-(1-imipazolyl)indolin-2-one
DE3714473A1 (en) 1987-04-30 1988-11-10 Basf Ag CONTINUOUS PROCESS FOR EPIMERIZING SUGAR, ESPECIALLY FROM D-ARABINOSE TO D-RIBOSE
RU2084449C1 (en) * 1994-03-02 1997-07-20 Всероссийский научный центр по безопасности биологически активных веществ 1-benzyl-2-oxotryptamine hydrochloride and its derivatives showing hepatoprotective activity
FR2740136B1 (en) 1995-10-24 1998-01-09 Sanofi Sa INDOLIN-2-ONE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
WO1998054167A1 (en) 1997-05-28 1998-12-03 Mitsubishi-Tokyo Pharmaceuticals, Inc. Indole compounds
US6511974B1 (en) * 1997-07-30 2003-01-28 Wyeth Tricyclic vasopressin agonists
EP0947511A1 (en) 1998-03-30 1999-10-06 F. Hoffmann-La Roche Ag Derivatives of phenoxy acetic acid and of phenoxymethyl tetrazole having antitumor activity
GB9819860D0 (en) 1998-09-12 1998-11-04 Zeneca Ltd Chemical compounds
JP2000191661A (en) 1998-12-25 2000-07-11 Mitsubishi-Tokyo Pharmaceuticals Inc Cyclic amide compound
BR0010482A (en) 1999-05-21 2002-04-23 Bristol Myers Squibb Co Pyrrolotriazinic kinase inhibitors
SK822002A3 (en) 1999-07-21 2002-09-10 Astrazeneca Ab New compounds
FR2827604B1 (en) 2001-07-17 2003-09-19 Sanofi Synthelabo NOVEL 1-PHENYLSULFONYL-1,3-DIHYDRO-2H-INDOL-2- ONE DERIVATIVES, A PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
CA2478172A1 (en) 2002-03-15 2003-09-25 Eli Lilly And Company Dihydroindol-2-one derivatives as steroid hormone nuclear receptor modulators
DE202004014849U1 (en) * 2004-09-23 2005-02-03 Trw Automotive Safety Systems Gmbh Device for determining an absolute angle of rotation
JP5125501B2 (en) 2005-01-28 2013-01-23 大正製薬株式会社 1,3-dihydro-2H-indol-2-one compound and pyrrolidin-2-one compound condensed with aromatic heterocycle
BRPI0609172A2 (en) 2005-02-22 2010-02-23 Univ Michigan mdm2 small molecule inhibitors and uses of these
US7576082B2 (en) 2005-06-24 2009-08-18 Hoffman-La Roche Inc. Oxindole derivatives
US20070213341A1 (en) 2006-03-13 2007-09-13 Li Chen Spiroindolinone derivatives
DE602007011902D1 (en) 2006-03-13 2011-02-24 Hoffmann La Roche SPIROINDOLINON DERIVATIVES
US7495007B2 (en) * 2006-03-13 2009-02-24 Hoffmann-La Roche Inc. Spiroindolinone derivatives
BRPI0713119A2 (en) 2006-06-30 2012-04-17 Schering Corp Substituted piperidines that increase the activity of p53 and the uses of these
MX2009002306A (en) 2006-08-30 2009-05-20 Univ Michigan New small molecule inhibitors of mdm2 and the uses thereof.
US7737174B2 (en) * 2006-08-30 2010-06-15 The Regents Of The University Of Michigan Indole inhibitors of MDM2 and the uses thereof
US7638548B2 (en) 2006-11-09 2009-12-29 Hoffmann-La Roche Inc. Spiroindolinone derivatives
WO2008080822A1 (en) 2006-12-29 2008-07-10 F. Hoffmann-La Roche Ag Epimerization methodologies for recovering stereo isomers in high yield and purity
US7553833B2 (en) * 2007-05-17 2009-06-30 Hoffmann-La Roche Inc. 3,3-spiroindolinone derivatives
US7776875B2 (en) 2007-12-19 2010-08-17 Hoffman-La Roche Inc. Spiroindolinone derivatives
US8258134B2 (en) 2008-04-16 2012-09-04 Hoffmann-La Roche Inc. Pyridazinone glucokinase activators
JP5658157B2 (en) * 2008-09-18 2015-01-21 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft Substituted pyrrolidine-2-carboxamide
US8354444B2 (en) * 2008-09-18 2013-01-15 Hoffmann-La Roche Inc. Substituted pyrrolidine-2-carboxamides
UA107814C2 (en) * 2009-11-12 2015-02-25 Дзе Ріджентс Оф Дзе Юніверсіті Оф Мічіган Spiro-oxindoles antagonists mdm 2
JP2013523820A (en) * 2010-04-09 2013-06-17 ザ、リージェンツ、オブ、ザ、ユニバーシティ、オブ、ミシガン Biomarkers of MDM2 inhibitors for use in treating diseases

Also Published As

Publication number Publication date
AU2010326855A1 (en) 2012-06-21
NZ600024A (en) 2014-08-29
ECSP12011945A (en) 2012-07-31
MA33976B1 (en) 2013-02-01
IL220010A (en) 2014-03-31
TW201129571A (en) 2011-09-01
AR079226A1 (en) 2012-01-04
CL2012001405A1 (en) 2012-09-28
SG181465A1 (en) 2012-07-30
KR20120101481A (en) 2012-09-13
ES2543468T3 (en) 2015-08-19
IL220010A0 (en) 2012-07-31
EP2507243A1 (en) 2012-10-10
BR112012012872A2 (en) 2017-10-10
AU2010326855B2 (en) 2015-10-29
US8088815B2 (en) 2012-01-03
US20110130398A1 (en) 2011-06-02
KR101418191B1 (en) 2014-07-09
RU2571100C2 (en) 2015-12-20
EP2507243B1 (en) 2015-06-10
JP5647262B2 (en) 2014-12-24
JP2013512869A (en) 2013-04-18
ZA201204036B (en) 2013-02-27
CA2781823A1 (en) 2011-06-09
RU2012125763A (en) 2014-01-10
MY160596A (en) 2017-03-15
PE20121334A1 (en) 2012-10-12
CN102741257A (en) 2012-10-17
CN102741257B (en) 2015-03-04
CR20120259A (en) 2012-07-12
MX2012006260A (en) 2012-06-19
HK1173720A1 (en) 2013-05-24
WO2011067185A1 (en) 2011-06-09

Similar Documents

Publication Publication Date Title
CO6541606A2 (en) ESPIROINDOLINONA- PIRROLIDINAS
CR20120410A (en) PIRROLIDINA-2-SUBSTITUTED CARBOXAMIDS
ECSP13013074A (en) NEW DERIVATIVES OF PIRIDINA
CO6361910A2 (en) PIRROLIDINA-2-SUBSTITUTED CARBOXAMIDS
CR20120443A (en) DERIVATIVES OF (IMIDAZOPIRIMIDINA-7-IL) -HETEROARILAMIDA AND ITS USE AS PDE10A INHIBITORS
CR20150250A (en) NEW DERIVATIVES OF PIRIDINA
CR20120594A (en) NITROGEN HETEROARILO COMPOUNDS
CO6630154A2 (en) Certain amino-pyridazines, compositions thereof and methods of use of pampering
CO6430459A2 (en) PROLIN DERIVATIVES AS CATEPSIN INHIBITORS
CR20150204A (en) NEW DERIVATIVES OF PIRIDINA
CO6620055A2 (en) Certain amino-pyrimidines, compositions thereof and methods for the use thereof
CO6741154A2 (en) Triazolopyridine Compounds
CR20150277A (en) PIRIDINA-2-USEFUL AMIDAS AS CB2 AGONISTS
CR20140399A (en) PIRROLIDINA-2-SUBSTITUTED CARBOXAMIDS
UY34365A (en) HETEROCICLICAL COMPOUNDS
CR20140079A (en) AMINOQUINAZOLINS AS QUINASE INHIBITORS
CU24078B1 (en) THREE RING SULFONAMID COMPOUNDS
UY32553A (en) NEW DERIVATIVES OF PIRROLIDINADIONA ESPIROHETEROCÍCLICOS 3-REPLACED
PA8779101A1 (en) "TRICYCLIC COMPOUNDS AS INHIBITORS OF MARRIAGE METALOPROTEINASES"
CR20110219A (en) NAPHYLACTIC ACIDS
NI201100096A (en) LACTAMS AS BETA SECRETASE INHIBITORS.
UY33176A (en) DERIVATIVES OF OXAZOLOPIRIMIDINE REPLACED IN 2, 5, 7.
CR20130318A (en) NEW BENZODIOXOL-PIPERAZINA COMPOUNDS
HN2009001330A (en) ACTIVE NEW NOVEDOUS COMPOUNDS AS MUSCARINIC RECEPTORE ANTAGONISTS
UY33180A (en) HETEROCYCLIC CARBOXYLIC ACID DERIVATIVES THAT INCLUDE A 2,5-REPLACED OXAZOLOPIRIMIDINE RING.

Legal Events

Date Code Title Description
FA Application withdrawn